Canonical Allele Identifier: CA1158981388

Gene: FUCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23848604_23848605delinsTG , CM000663.2:g.23848604_23848605delinsTG	GRCh38
NC_000001.10:g.24175094_24175095delinsTG , CM000663.1:g.24175094_24175095delinsTG	GRCh37
NC_000001.9:g.24047681_24047682delinsTG	NCBI36
NG_013346.1:g.24765_24766delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374479.4:c.1160+44_1160+45delinsCA MANE Select	ENSP00000363603.3:n.1160+44_1160+45delinsCA
ENST00000374479.3:c.1160+44_1160+45delinsCA	ENSP00000363603.3:n.1160+44_1160+45delinsCA
NM_000147.4:c.1160+44_1160+45delinsCA	NP_000138.2:n.1160+44_1160+45delinsCA
XM_005245821.1:c.785+44_785+45delinsCA	XP_005245878.1:n.785+44_785+45delinsCA
XM_011541167.1:c.527+44_527+45delinsCA	XP_011539469.1:n.527+44_527+45delinsCA
XM_005245821.3:c.785+44_785+45delinsCA	XP_005245878.1:n.785+44_785+45delinsCA
XM_011541167.3:c.527+44_527+45delinsCA	XP_011539469.1:n.527+44_527+45delinsCA
XM_017000905.2:c.857+44_857+45delinsCA	XP_016856394.1:n.857+44_857+45delinsCA
NM_000147.5:c.1160+44_1160+45delinsCA MANE Select	NP_000138.2:n.1160+44_1160+45delinsCA
NR_174379.1:n.1338+44_1338+45delinsCA
NR_174380.1:n.1387+44_1387+45delinsCA
NR_174381.1:n.1226+44_1226+45delinsCA
NR_174382.1:n.1623+44_1623+45delinsCA